A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461667



Internal ID22519552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33152800..33154699hg38UCSC Ensembl
chr1:33618401..33620300hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829998
Supporting Variants
Samples
Known GenesTRIM62
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461667
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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